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Company Name Brand Name GMDN Term Name GMDN Term Status FDA Product Code Name FDA Product Code Device Packaged As Sterile Sterilization Prior To Use Issuing Agency Device Size Device Class Implantable

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VuePoint II Trial, 25mmx0° Lat Offst Con
Nuvasive, Inc.
8976173
In Commercial Distribution

  • 00887517884633 ()


  • Internal spinal fixation procedure kit, reusable
VuePoint II Trial, 11mmx0° Lat Offst Con
Nuvasive, Inc.
8976170
In Commercial Distribution

  • 00887517884602 ()


  • Internal spinal fixation procedure kit, reusable
Modulus XLW 5° Movers Sterile
Nuvasive, Inc.
MDLUSXLW5
In Commercial Distribution

  • 00887517884534 ()


  • Device sterilization/disinfection container, reusable
Modulus TLIF-O, 14x10x30mm 8°
Nuvasive, Inc.
2140308P2
In Commercial Distribution

  • 00887517883896 ()


  • Metallic spinal interbody fusion cage
Modulus TLIF-O, 14x10x30mm 4°
Nuvasive, Inc.
2140304P2
In Commercial Distribution

  • 00887517883858 ()


  • Metallic spinal interbody fusion cage
Modulus TLIF-O, 14x10x30mm 12°
Nuvasive, Inc.
2140302P2
In Commercial Distribution

  • 00887517883834 ()


  • Metallic spinal interbody fusion cage
Modulus TLIF-O, 14x10x25mm 8°
Nuvasive, Inc.
2140258P2
In Commercial Distribution

  • 00887517883797 ()


  • Metallic spinal interbody fusion cage
Modulus TLIF-O, 14x10x25mm 4°
Nuvasive, Inc.
2140254P2
In Commercial Distribution

  • 00887517883759 ()


  • Metallic spinal interbody fusion cage
Modulus TLIF-O, 14x10x25mm 12°
Nuvasive, Inc.
2140252P2
In Commercial Distribution

  • 00887517883735 ()


  • Metallic spinal interbody fusion cage
Modulus TLIF-O, 12x14x30mm 4°
Nuvasive, Inc.
2124304P2
In Commercial Distribution

  • 00887517882653 ()


  • Metallic spinal interbody fusion cage
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